A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444521



Internal ID22502391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80200763..80204266hg38UCSC Ensembl
chr9:82815678..82819181hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg383504
hg193504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444521
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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